Apollo Adlux Hospital’s Fetal and Reproductive Genetics services support couples and families who require genetic evaluation before, during, or after pregnancy. Comprehensive genetic assessment can help identify potential genetic risks, evaluate fetal anomalies, and provide informed guidance regarding prenatal and reproductive decisions. Clinical geneticists and genetic counsellors help families understand available testing options and their implications.

Fetal anomaly evaluation forms an important component of prenatal genetics. Ultrasound findings suggesting structural abnormalities, growth concerns, or other fetal anomalies may require further genetic assessment. Prenatal genetic counselling can help determine whether non-invasive or invasive genetic testing is appropriate based on the clinical situation and family history.

Preconception counselling provides couples with an opportunity to understand potential inherited disease risks before pregnancy. Recurrent pregnancy loss and infertility evaluation may also benefit from genetic assessment when an underlying chromosomal or genetic factor is suspected.

Non-invasive prenatal testing (NIPT) offers screening for selected chromosomal abnormalities, while invasive diagnostic procedures such as chorionic villus sampling (CVS) and amniocentesis can provide samples for definitive genetic testing when clinically indicated. Apollo Adlux Medical Genetics provides guidance regarding these testing options, helping families understand benefits, limitations, possible outcomes, and appropriate follow-up.

Personalised genetic counselling remains central to fetal and reproductive genetics, supporting informed and responsible reproductive decision-making.